FindTrial
Sign In

Clinical study on prevention of cervical adhesion after loop electrosurgical excision procedure (LEEP)

Clinical study on prevention of cervical adhesion after loop electrosurgical excision procedure (LEEP)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800017629
Enrollment
Unknown
Registered
2018-08-07
Start date
2018-09-01
Completion date
Unknown
Last updated
2018-08-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervical disease

Interventions

1:Non intervention
2:Dilation of the cervix third, fifth, eighth weeks after the operation
3:Dilation of the cervix in the first, second, and third postoperatively

Sponsors

International Peace Maternity & Child Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
42 Years to 72 Years

Inclusion criteria

Inclusion criteria: 1. age: patient over 45 years after LEEP. The first group: over 45 years old to menopause <1 years; the second group: menopause is more than 1 years. 2. Patient who needs to be followed up after LEEP.

Exclusion criteria

Exclusion criteria: 1. patient diagnosed as cervical cancer by pathology after LEEP, and needs to accept hysterectomy or hysterectomy; 2. the patient who will be unable to follow up.

Design outcomes

Primary

MeasureTime frame
Degree of cervical adhesion;—

Countries

China

Contacts

Public ContactWu Dan

International Peace Maternity & Child Health Hospital

wudan2017@yeah.net+86 18017316126

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026